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Comprehensive Program for Youth Mental Health

Comprehensive Program for Youth Mental Health

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02169960
Acronym
EMPATHY
Enrollment
5514
Registered
2014-06-23
Start date
2014-02-28
Completion date
2015-06-30
Last updated
2015-12-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Suicide

Brief summary

The majority of addiction and mental health problems seen in adults present first in youth. There is strong evidence that prevention and early identification during childhood can mitigate some of these risks. Students who screen at risk for the development of mental illness will be offered online intervention programs with personal guidance from a trained coach. In addition, lessons revolving around resiliency will be provided to all students. The objectives of this study are: * Decreased rates of depression and suicide (as well as rates of suicide attempts) * Decreased use of alcohol, tobacco, and other drugs, with additional downstream benefits such as reduced rates of fetal alcohol spectrum disorder (FASD) and cancer * Decreased school drop-out rates Decreased rates of interactions with the justice system * Decreased costs across a range of ministries (health, education, justice, human services), both for youth as well as their families who have been involved in this program

Interventions

BEHAVIORALSmart, Positive, Active, Realistic X-factor thoughts (SPARX)

Cognitive Behavioral Therapy based online intervention for depression

BEHAVIORALBreaking Free

Online based intervention for Drug and Alcohol Use

BEHAVIORALThis Way Up

Cognitive Behavioral Therapy online intervention for Depression and Anxiety

Op Volle Kracht (OVK)

Sponsors

Red Deer Public School District
CollaboratorOTHER
Addiction & Mental Health Strategic Clinical Network
CollaboratorOTHER
University of Alberta
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
11 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* The intervention group will be the top 10% of all students participating in the school screening.

Exclusion criteria

* Lack of consent, lack of assent, lack of the ability to read and understand the screening tools or intervention tools

Design outcomes

Primary

MeasureTime frameDescription
Decrease from baseline in rates of depression and suicide12 monthsThis will be based on scores on the Patient Health Questionnaire for Adolescents (PHQ-A) questionnaire

Secondary

MeasureTime frameDescription
Decreased use of alcohol, tobacco and other drugsBaseline, 3 months, 6 months, 12 monthsQuestionnaire (CRAFFT)
Decreased school drop-out rates12 monthsWill be tracking the School identification numbers of the students in order to determine how many drop out prior to graduation. This will be compared with historical data from Red Deer Public Schools.
Decreased rates of interactions with the justice system12 monthsWill be linking with a data groups' repository as well as ministries in order to determine rates of interactions with the justice system.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026